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Full genome SNP-based phylogenetic analysis reveals the origin and global spread of Brucella melitensis

BACKGROUND: Brucellosis is an important zoonotic disease that affects both humans and animals. We sequenced the full genome and characterised the genetic diversity of two Brucella melitensis isolates from Malaysia and the Philippines. In addition, we performed a comparative whole-genome single nucle...

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Autores principales: Tan, Kim-Kee, Tan, Yung-Chie, Chang, Li-Yen, Lee, Kok Wei, Nore, Siti Sarah, Yee, Wai-Yan, Mat Isa, Mohd Noor, Jafar, Faizatul Lela, Hoh, Chee-Choong, AbuBakar, Sazaly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409723/
https://www.ncbi.nlm.nih.gov/pubmed/25888205
http://dx.doi.org/10.1186/s12864-015-1294-x
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author Tan, Kim-Kee
Tan, Yung-Chie
Chang, Li-Yen
Lee, Kok Wei
Nore, Siti Sarah
Yee, Wai-Yan
Mat Isa, Mohd Noor
Jafar, Faizatul Lela
Hoh, Chee-Choong
AbuBakar, Sazaly
author_facet Tan, Kim-Kee
Tan, Yung-Chie
Chang, Li-Yen
Lee, Kok Wei
Nore, Siti Sarah
Yee, Wai-Yan
Mat Isa, Mohd Noor
Jafar, Faizatul Lela
Hoh, Chee-Choong
AbuBakar, Sazaly
author_sort Tan, Kim-Kee
collection PubMed
description BACKGROUND: Brucellosis is an important zoonotic disease that affects both humans and animals. We sequenced the full genome and characterised the genetic diversity of two Brucella melitensis isolates from Malaysia and the Philippines. In addition, we performed a comparative whole-genome single nucleotide polymorphism (SNP) analysis of B. melitensis strains collected from around the world, to investigate the potential origin and the history of the global spread of B. melitensis. RESULTS: Single sequencing runs of each genome resulted in draft genome sequences of MY1483/09 and Phil1136/12, which covered 99.85% and 99.92% of the complete genome sequences, respectively. The B. melitensis genome sequences, and two B. abortus strains used as the outgroup strains, yielded a total of 13,728 SNP sites. Phylogenetic analysis using whole-genome SNPs and geographical distribution of the isolates revealed spatial clustering of the B. melitensis isolates into five genotypes, I, II, III, IV and V. The Mediterranean strains, identified as genotype I, occupied the basal node of the phylogenetic tree, suggesting that B. melitensis may have originated from the Mediterranean regions. All of the Asian B. melitensis strains clustered into genotype II with the SEA strains, including the two isolates sequenced in this study, forming a distinct clade denoted here as genotype IId. Genotypes III, IV and V of B. melitensis demonstrated a restricted geographical distribution, with genotype III representing the African lineage, genotype IV representing the European lineage and genotype V representing the American lineage. CONCLUSION: We showed that SNPs retrieved from the B. melitensis draft full genomes were sufficient to resolve the interspecies relationships between B. melitensis strains and to discriminate between the vaccine and endemic strains. Phylogeographic reconstruction of the history of B. melitensis global spread at a finer scale by using whole-genome SNP analyses supported the origin of all B. melitensis strains from the Mediterranean region. The possible global distribution of B. melitensis following the ancient trade routes was also consistent with whole-genome SNP phylogeny. The whole genome SNP phylogenetics analysis, hence is a powerful tool for intraspecies discrimination of closely related species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1294-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-44097232015-04-26 Full genome SNP-based phylogenetic analysis reveals the origin and global spread of Brucella melitensis Tan, Kim-Kee Tan, Yung-Chie Chang, Li-Yen Lee, Kok Wei Nore, Siti Sarah Yee, Wai-Yan Mat Isa, Mohd Noor Jafar, Faizatul Lela Hoh, Chee-Choong AbuBakar, Sazaly BMC Genomics Research Article BACKGROUND: Brucellosis is an important zoonotic disease that affects both humans and animals. We sequenced the full genome and characterised the genetic diversity of two Brucella melitensis isolates from Malaysia and the Philippines. In addition, we performed a comparative whole-genome single nucleotide polymorphism (SNP) analysis of B. melitensis strains collected from around the world, to investigate the potential origin and the history of the global spread of B. melitensis. RESULTS: Single sequencing runs of each genome resulted in draft genome sequences of MY1483/09 and Phil1136/12, which covered 99.85% and 99.92% of the complete genome sequences, respectively. The B. melitensis genome sequences, and two B. abortus strains used as the outgroup strains, yielded a total of 13,728 SNP sites. Phylogenetic analysis using whole-genome SNPs and geographical distribution of the isolates revealed spatial clustering of the B. melitensis isolates into five genotypes, I, II, III, IV and V. The Mediterranean strains, identified as genotype I, occupied the basal node of the phylogenetic tree, suggesting that B. melitensis may have originated from the Mediterranean regions. All of the Asian B. melitensis strains clustered into genotype II with the SEA strains, including the two isolates sequenced in this study, forming a distinct clade denoted here as genotype IId. Genotypes III, IV and V of B. melitensis demonstrated a restricted geographical distribution, with genotype III representing the African lineage, genotype IV representing the European lineage and genotype V representing the American lineage. CONCLUSION: We showed that SNPs retrieved from the B. melitensis draft full genomes were sufficient to resolve the interspecies relationships between B. melitensis strains and to discriminate between the vaccine and endemic strains. Phylogeographic reconstruction of the history of B. melitensis global spread at a finer scale by using whole-genome SNP analyses supported the origin of all B. melitensis strains from the Mediterranean region. The possible global distribution of B. melitensis following the ancient trade routes was also consistent with whole-genome SNP phylogeny. The whole genome SNP phylogenetics analysis, hence is a powerful tool for intraspecies discrimination of closely related species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1294-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-18 /pmc/articles/PMC4409723/ /pubmed/25888205 http://dx.doi.org/10.1186/s12864-015-1294-x Text en © Tan et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Tan, Kim-Kee
Tan, Yung-Chie
Chang, Li-Yen
Lee, Kok Wei
Nore, Siti Sarah
Yee, Wai-Yan
Mat Isa, Mohd Noor
Jafar, Faizatul Lela
Hoh, Chee-Choong
AbuBakar, Sazaly
Full genome SNP-based phylogenetic analysis reveals the origin and global spread of Brucella melitensis
title Full genome SNP-based phylogenetic analysis reveals the origin and global spread of Brucella melitensis
title_full Full genome SNP-based phylogenetic analysis reveals the origin and global spread of Brucella melitensis
title_fullStr Full genome SNP-based phylogenetic analysis reveals the origin and global spread of Brucella melitensis
title_full_unstemmed Full genome SNP-based phylogenetic analysis reveals the origin and global spread of Brucella melitensis
title_short Full genome SNP-based phylogenetic analysis reveals the origin and global spread of Brucella melitensis
title_sort full genome snp-based phylogenetic analysis reveals the origin and global spread of brucella melitensis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409723/
https://www.ncbi.nlm.nih.gov/pubmed/25888205
http://dx.doi.org/10.1186/s12864-015-1294-x
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